Evaluation of reference genes for transcript analyses in Komagataella phaffii (Pichia pastoris).

Q1 Agricultural and Biological Sciences
Mihail Besleaga, Gabriel A Vignolle, Julian Kopp, Oliver Spadiut, Robert L Mach, Astrid R Mach-Aigner, Christian Zimmermann
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引用次数: 1

Abstract

Background: The yeast Komagataella phaffii (Pichia pastoris) is routinely used for heterologous protein expression and is suggested as a model organism for yeast. Despite its importance and application potential, no reference gene for transcript analysis via RT-qPCR assays has been evaluated to date. In this study, we searched publicly available RNASeq data for stably expressed genes to find potential reference genes for relative transcript analysis by RT-qPCR in K. phaffii. To evaluate the applicability of these genes, we used a diverse set of samples from three different strains and a broad range of cultivation conditions. The transcript levels of 9 genes were measured and compared using commonly applied bioinformatic tools.

Results: We could demonstrate that the often-used reference gene ACT1 is not very stably expressed and could identify two genes with outstandingly low transcript level fluctuations. Consequently, we suggest the two genes, RSC1, and TAF10 to be simultaneously used as reference genes in transcript analyses by RT-qPCR in K. phaffii in future RT-qPCR assays.

Conclusion: The usage of ACT1 as a reference gene in RT-qPCR analysis might lead to distorted results due to the instability of its transcript levels. In this study, we evaluated the transcript levels of several genes and found RSC1 and TAF10 to be extremely stable. Using these genes holds the promise for reliable RT-qPCR results.

Abstract Image

法菲氏酵母(Pichia pastoris)转录本分析内参基因的评价。
背景:酵母法菲Komagataella phaffii(毕赤酵母)通常用于异种蛋白的表达,被认为是酵母的一种模式生物。尽管它的重要性和应用潜力,但迄今为止还没有评估过RT-qPCR分析转录本的参考基因。在本研究中,我们从公开的RNASeq数据中寻找稳定表达的基因,寻找潜在的内参基因,进行相对转录分析。为了评估这些基因的适用性,我们使用了来自三种不同菌株的不同样本和广泛的培养条件。利用常用的生物信息学工具对9个基因的转录水平进行了测定和比较。结果:我们可以证明常用的内参基因ACT1表达不是很稳定,可以鉴定两个转录水平波动非常低的基因。因此,我们建议在未来的RT-qPCR分析中,RSC1和TAF10两个基因同时作为法菲氏K.的转录本分析的内参基因。结论:使用ACT1作为内参基因进行RT-qPCR分析可能会由于其转录水平的不稳定性导致结果失真。在这项研究中,我们评估了几个基因的转录水平,发现RSC1和TAF10是非常稳定的。使用这些基因有望获得可靠的RT-qPCR结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Fungal Biology and Biotechnology
Fungal Biology and Biotechnology Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
10.20
自引率
0.00%
发文量
17
审稿时长
9 weeks
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